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Transungual Drug Delivery: An Overview
Transungual Drug Delivery: An Overview

... Physical, chemical and mechanical methods have been used to decrease the nail barrier. Within each of these broad categories, many techniques exist to enhance penetration. Mechanical modes of penetration enhancement are typically straightforward, and have the most in vivo experience associated with ...
4 Aqueous Extract of Human Placenta as a Therapeutic Agent Piyali Datta Chakraborty
4 Aqueous Extract of Human Placenta as a Therapeutic Agent Piyali Datta Chakraborty

... on the extract has highlighted some important components that might play roles in this process while few more are yet to be identified. Once the active components are identified and a proper biochemical basis of their action is defined, these components may be used even for newer purposes (Chakrabor ...
the simultaneous determination of candesartan
the simultaneous determination of candesartan

... improves the ratio cost-effectiveness of treatment and patient's compliance [7, 15]. Combined therapy with calcium channel blockers, angiotensin II blockers and diuretics is recommended as one of the most effective and commonly used to treat hypertension [3, 10]. ...
Review On The Medicinial Plant - Aerva Lanata
Review On The Medicinial Plant - Aerva Lanata

... group comprise approximately 8000 species and account for about 50% of all the higher flowering plant species in India. The knowledge of medicinal plants has been accumulated in the course of many centuries based on different medicinal systems such as Ayurveda, Unani and Siddha. In large number of c ...
EBOLA and FDA: reviewing the response to the 2014 outbreak, to
EBOLA and FDA: reviewing the response to the 2014 outbreak, to

... While there are many lenses through which one might examine and critique the unfolding of and response to the 2014 Ebola outbreak, this paper adopts the lens of food and drug law and focuses on the significant role assumed by the U.S. Food and Drug Administration (FDA). Because there were no FDA-app ...
AusPAR: Sevelamer hydrochloride
AusPAR: Sevelamer hydrochloride

... The limits and tests for identification, chloride content, water soluble oligomers, allylamine content, epichlorohydrin content and particle size are in line or tighter than those specified in the draft USP monograph for sevelamer hydrochloride. All of the tests have been adequately described and we ...
Meperidine - Home - KSU Faculty Member websites
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... • Meperidine or pethidine is a narcotic analgesic Introduced in the 1930s, it produces effects that are similar, but not identical, to morphine (shorter duration of action and reduced antitussive and antidiarrheal actions). ...
Fengyan Jin1*, Wei Li1, Joel G. Turner
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... anti-angiogenesis as a potential anti-cancer therapy due to dependency of solid tumors on angiogenesis induced by a factor secreted from these tumors, and his colleagues discovered that thalidomide functions as an inhibitor of angiogenesis triggered by basic fibroblast growth factor in a rabbit corn ...
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... The concurrent use of latex condoms or diaphragms with vaginal anti-infective preparations may decrease the effectiveness of latex contraceptive agents. Therefore, GYNO-DAKTARIN products should not be used concurrently with a latex condom or latex diaphragm. Interactions with Other Medicinal Product ...
Diminished Cocaine-Like Effects in Dopamine Transporter Ligands
Diminished Cocaine-Like Effects in Dopamine Transporter Ligands

... dopamine uptake will have behavioral effects like those of cocaine (Kuhar et al., 1991). In addition, an understanding of the differences in pharmacological mechanisms of cocaine and the BZT analogs may provide insight into the neurobiological substrates that underlie the abuse liability of cocaine ...
Approved Drug Utilization Review Board Edits
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...  For adolescents age 13 years through 17 years and adults age 18 years and older who meet the adult ADD/ADHD or narcolepsy criteria, a once daily dose of 72 mg for methylphenidate extended release tablets (e.g., Concerta®) may be requested through the manual review PA process by submitting a letter ...
10 November 2014 EMA/CHMP/SAWP/72894/2008 Revision 1: January 2012
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... Qualification advice for future studies: The report of the qualification team may recommend adopting a qualification advice on future studies to be performed in order to generate the data required to support the proposed context of use of the method in drug development. This outcome is envisaged for ...
Patient Registries and Participating in Clinical Trials
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... Trial Must Make It Accessible To All Ataxia Patients. • Design trials that can use the fewest patients over the shortest period of time (this usually means testing better drugs and using biomarkers). • What is the rationale for excluding certain patients? Can those excluded be used in other ways? Pa ...
A REVIEW ON ANALYTICAL METHODOLOGIES FOR THE DETERMINATION OF PIPERACILLIN
A REVIEW ON ANALYTICAL METHODOLOGIES FOR THE DETERMINATION OF PIPERACILLIN

... injection; piperacillin/tazobactam is administered intravenously every 6 or 8 hours; the drug may also be given by continuous infusion. It has been shown that the bacteriocidal actions of the drug do not increase with concentrations of piperacillin higher than 46xMIC, which means that the drug is co ...
CALOTROPIS  PROCERA Research Article   
CALOTROPIS  PROCERA Research Article   

... The  methanolic  extract  of  plant  Calotropis  procera  (Asclepiadaceae),  has  been  reported  to  exhibit  potent  anti‐inflammatory  activity  against  carrageenan induced paw oedema and cotton pellet induced granuloma in albino Wistar rats. In the present study we have evaluated the efficacy o ...
UPDATE OF CANNABIS BACKGROUND PAPER
UPDATE OF CANNABIS BACKGROUND PAPER

... explanations which have been put forward by observers are discriminatory behaviour by law enforcement personnel, and/or people in low socio-economic groups having more incentive to engage in lucrative illegal activity. Official data demonstrates that Mäori are more likely to have lower incomes, high ...
Map and Application of States That Require a Prescription for
Map and Application of States That Require a Prescription for

... Exempts Bronkaid· Caplets and Primatene· Tablets because they are approved for sale over the counter without a prescription under federal law, are labeled and marketed in a manner consistent with the pertinent OTC tentative final or final monograph, are manufactured and distributed for legitimate me ...
Antipsychotic Drugs - Pharmacological Reviews
Antipsychotic Drugs - Pharmacological Reviews

... shows that the selectivity is low and had been overestimated previously owing to overestimation of the Ki at the D2 receptor when determined in competition versus [3H]spiperone. Problems with the use of high-affinity ligands can also be seen in the in vivo scanning techniques. For example, some of t ...
Map and Application of States That Require a Prescription for
Map and Application of States That Require a Prescription for

... Exempts Bronkaid· Caplets and Primatene· Tablets because they are approved for sale over the counter without a prescription under federal law, are labeled and marketed in a manner consistent with the pertinent OTC tentative final or final monograph, are manufactured and distributed for legitimate me ...
IJCT 13(4) 360-366
IJCT 13(4) 360-366

... measured excess of bromate-bromide reagent in acid medium to CPH, and after the reaction is ensured to be complete, the residual bromine is determined by reacting with a fixed amount of methyl orange, and measuring the absorbance at 520 nm. In kinetic method, a mixture containing CPH and methyl oran ...
QbD terminology - Parenterals 2015
QbD terminology - Parenterals 2015

... administered in a manner other than through the digestive tract, as by intravenous or intramuscular injection.  Most effective and common form of delivery for active drug substances with metabolic bio-availabilities drug for which the bioavailability in limited by high first pass metabolism effect ...
Newer Antihistamines
Newer Antihistamines

... activity'. In this two-state model, histamine acts as an agonist by combining with and stabilizing the activated conformation of the H1-receptor to shift the equilibrium towards the activated state. Drugs classified previously as antagonists act as either inverse agonists or neutral antagonists. Inv ...
Key Test Findings Affiliated Genetics
Key Test Findings Affiliated Genetics

... The assays detect alleles listed above, including all common and most rare variants with known clinical significance at analytical  sensitivity and specificity >99%. Limitations: The interpretations provided in this report are provided to assist health care providers, but they are not a treatment  r ...
Drug Wars - National Center for Case Study Teaching in Science
Drug Wars - National Center for Case Study Teaching in Science

... Ten-year-old Leia was taken to the on-call pediatric clinic that collaborates with her pediatrician’s office after a rough night of little sleep with severe wheezing and a frequent, dry cough. During the night, her mother had given Leia albuterol and fluticasone approximately every four hours using ...
Filters and Filtration: A Review of Mechanisms That Impact Cost
Filters and Filtration: A Review of Mechanisms That Impact Cost

... construction are available for use in various applications. The wide variety and type of filters available today also mean that we do not completely understand the nature of such filters and random or un-informed usage could introduce unwanted alterations in the quality or quantity of the product. T ...
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Drug discovery



In the fields of medicine, biotechnology and pharmacology, drug discovery is the process by which new candidate medications are discovered. Historically, drugs were discovered through identifying the active ingredient from traditional remedies or by serendipitous discovery. Later chemical libraries of synthetic small molecules, natural products or extracts were screened in intact cells or whole organisms to identify substances that have a desirable therapeutic effect in a process known as classical pharmacology. Since sequencing of the human genome which allowed rapid cloning and synthesis of large quantities of purified proteins, it has become common practice to use high throughput screening of large compounds libraries against isolated biological targets which are hypothesized to be disease modifying in a process known as reverse pharmacology. Hits from these screens are then tested in cells and then in animals for efficacy.Modern drug discovery involves the identification of screening hits, medicinal chemistry and optimization of those hits to increase the affinity, selectivity (to reduce the potential of side effects), efficacy/potency, metabolic stability (to increase the half-life), and oral bioavailability. Once a compound that fulfills all of these requirements has been identified, it will begin the process of drug development prior to clinical trials. One or more of these steps may, but not necessarily, involve computer-aided drug design. Modern drug discovery is thus usually a capital-intensive process that involves large investments by pharmaceutical industry corporations as well as national governments (who provide grants and loan guarantees). Despite advances in technology and understanding of biological systems, drug discovery is still a lengthy, ""expensive, difficult, and inefficient process"" with low rate of new therapeutic discovery. In 2010, the research and development cost of each new molecular entity (NME) was approximately US$1.8 billion. Drug discovery is done by pharmaceutical companies, with research assistance from universities. The ""final product"" of drug discovery is a patent on the potential drug. The drug requires very expensive Phase I, II and III clinical trials, and most of them fail. Small companies have a critical role, often then selling the rights to larger companies that have the resources to run the clinical trials.Discovering drugs that may be a commercial success, or a public health success, involves a complex interaction between investors, industry, academia, patent laws, regulatory exclusivity, marketing and the need to balance secrecy with communication. Meanwhile, for disorders whose rarity means that no large commercial success or public health effect can be expected, the orphan drug funding process ensures that people who experience those disorders can have some hope of pharmacotherapeutic advances.
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